Funds are requested to set up a truly national Resource for protein crystallography. This Resource will house two high speed data collection systems which will be available to protein crystallography groups in the United States. The first system which presently consists of a standard, fixed-source X-ray generator and one multiwire area X-ray detector can, as has been demonstrated, collect data about 10 times faster than a standard diffractometer and can collect data efficiently for protein crystals with unit cell dimensions up to about 120 Angstroms. The second system consisting of a rotating anode X-ray source and up to 6 or more area detectors will be at least one hundred times faster than a standard diffractometer and will be able to collect data efficiently for protein crystals with unit cell dimensions up to 300 to 400 Angstroms. This resource will be directed by an advisory board composed of well known protein crystallographers and biochemists from all regions of the United States. This board will provide scientific direction, establish the Resource guidelines and assure equitable access to the Resource by all user groups. Core researches wil also be an improtant activity of the resource since one of its aims is to continue to develop better area detectors and better methods to collect protein crystallographic data. The third important activity of the resource is the training of other protein crystallographers on the new methods of data collection, therefore every two years the resource staff will set up workshops and seminars on this subject. Protection crystallographers are also encouraged to spend a short period of time (about one month) at the resource in order to get some hand-on experience.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001644-08
Application #
3103965
Study Section
Special Emphasis Panel (SSS (E))
Project Start
1983-07-01
Project End
1991-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
8
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Biswas, Saswati; Biswas, Indranil (2011) Role of VltAB, an ABC transporter complex, in viologen tolerance in Streptococcus mutans. Antimicrob Agents Chemother 55:1460-9
Chattoraj, Partho; Banerjee, Anirban; Biswas, Saswati et al. (2010) ClpP of Streptococcus mutans differentially regulates expression of genomic islands, mutacin production, and antibiotic tolerance. J Bacteriol 192:1312-23
Grimplet, Jérôme; Wheatley, Matthew D; Jouira, Hatem Ben et al. (2009) Proteomic and selected metabolite analysis of grape berry tissues under well-watered and water-deficit stress conditions. Proteomics 9:2503-28
Zhang, Jiaqin; Biswas, Indranil (2009) 3'-Phosphoadenosine-5'-phosphate phosphatase activity is required for superoxide stress tolerance in Streptococcus mutans. J Bacteriol 191:4330-40
Drummond, Christopher S (2008) Diversification of Lupinus (Leguminosae) in the western New World: derived evolution of perennial life history and colonization of montane habitats. Mol Phylogenet Evol 48:408-21
Althoff, David M (2008) A test of host-associated differentiation across the 'parasite continuum'in the tri-trophic interaction among yuccas, bogus yucca moths, and parasitoids. Mol Ecol 17:3917-27
Wickstrum, Jason R; Hong, Kee-Jong; Bokhari, Sirosh et al. (2007) Coactivating signals for the hepatic lymphocyte gamma interferon response to Francisella tularensis. Infect Immun 75:1335-42
Hong, Kee-Jong; Wickstrum, Jason R; Yeh, Hung-Wen et al. (2007) Toll-like receptor 2 controls the gamma interferon response to Francisella tularensis by mouse liver lymphocytes. Infect Immun 75:5338-45
Fan, G Y; Datte, P; Beuville, E et al. (1998) ASIC-based event-driven 2D digital electron counter for TEM imaging. Ultramicroscopy 70:107-13
Narayana, N; Cox, S; Nguyen-huu, X et al. (1997) A binary complex of the catalytic subunit of cAMP-dependent protein kinase and adenosine further defines conformational flexibility. Structure 5:921-35

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